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Alms1-disrupted mice recapitulate human Alström syndrome.
Collin GB, Cyr E, Bronson R, Marshall JD, Gifford EJ, Hicks W, Murray SA, Zheng QY, Smith RS, Nishina PM, Naggert JK. Collin GB, et al. Hum Mol Genet. 2005 Aug 15;14(16):2323-33. doi: 10.1093/hmg/ddi235. Epub 2005 Jul 6. Hum Mol Genet. 2005. PMID: 16000322 Free PMC article.
Fine Mapping of a Deafness Mutation hml on Mouse Chromosome 10.
Zheng QY, Harris BS, Ward-Bailey PF, Yu H, Bronson RT, Davisson MT, Johnson KR. Zheng QY, et al. Among authors: bronson rt. Acad J Xian Jiaotong Univ. 2004 Jun;25(3):209-212. Acad J Xian Jiaotong Univ. 2004. PMID: 21179397 Free PMC article.
Mutations in a P-type ATPase gene cause axonal degeneration.
Zhu X, Libby RT, de Vries WN, Smith RS, Wright DL, Bronson RT, Seburn KL, John SW. Zhu X, et al. Among authors: bronson rt. PLoS Genet. 2012;8(8):e1002853. doi: 10.1371/journal.pgen.1002853. Epub 2012 Aug 9. PLoS Genet. 2012. PMID: 22912588 Free PMC article.
A subset of p53-deficient embryos exhibit exencephaly.
Sah VP, Attardi LD, Mulligan GJ, Williams BO, Bronson RT, Jacks T. Sah VP, et al. Among authors: bronson rt. Nat Genet. 1995 Jun;10(2):175-80. doi: 10.1038/ng0695-175. Nat Genet. 1995. PMID: 7663512
544 results